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F Ballesta

Showing results (31-40 of 70) with videos related to

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American Journal of Medical Genetics|December 22, 1999
SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphroditeE Margarit, M D Coll, R Oliva, et al.
Neurology|February 20, 1999
A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizuresM Ezquerra, C Carnero, R Blesa, et al.
Acta Otorrinolaringologica Espanola|September 1, 1988
[Origin and distribution of nerve fibers immunoreacting with calcitonin gene-related peptide (CGRP) in the nasal respiratory mucosa in mammals]A E Amores, C Sprekelsen, J F Ballesta, et al.
Archives of Andrology|May 8, 2001
Chromosomal abnormalities and polymorphisms in infertile menS Penna Videaú, H Araujo, F Ballesta, et al.
Anales Espanoles De Pediatria|November 1, 1989
[Ring chromosome 17 and recurring pneumopathy]N Lambruschini Ferri, M E Ortola Castells, J Rosell Andreo, et al.
Clinical Genetics|June 15, 2005
Mutation analysis of Wilson disease in the Spanish population -- identification of a prevalent substitution and eight novel mutations in the ATP7B geneE Margarit, V Bach, D Gómez, et al.
Sangre|January 1, 1981
[Blast crisis mimicking acute leukaemia as first manifestations of chronic myelogenous leukaemia. Report of three cases (author's transl)]F Cervantes, C Rozman, F Ballesta, et al.
American Journal of Medical Genetics|March 10, 2000
Paternal isodisomy 13 in a normal newborn infant after trisomy rescue evidenced by prenatal diagnosisA Soler, E Margarit, R Queralt, et al.
Medicina Clinica|July 30, 1999
[Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome]M Milà, A Carrió, A Sánchez, et al.
Biochemical and Biophysical Research Communications|May 8, 1998
Identification of conserved potentially regulatory sequences of the SRY gene from 10 different species of mammalsE Margarit, A Guillén, C Rebordosa, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics|December 22, 1999
SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphroditeE Margarit, M D Coll, R Oliva, et al.
Neurology|February 20, 1999
A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizuresM Ezquerra, C Carnero, R Blesa, et al.
Acta Otorrinolaringologica Espanola|September 1, 1988
[Origin and distribution of nerve fibers immunoreacting with calcitonin gene-related peptide (CGRP) in the nasal respiratory mucosa in mammals]A E Amores, C Sprekelsen, J F Ballesta, et al.
Archives of Andrology|May 8, 2001
Chromosomal abnormalities and polymorphisms in infertile menS Penna Videaú, H Araujo, F Ballesta, et al.
Anales Espanoles De Pediatria|November 1, 1989
[Ring chromosome 17 and recurring pneumopathy]N Lambruschini Ferri, M E Ortola Castells, J Rosell Andreo, et al.
Clinical Genetics|June 15, 2005
Mutation analysis of Wilson disease in the Spanish population -- identification of a prevalent substitution and eight novel mutations in the ATP7B geneE Margarit, V Bach, D Gómez, et al.
Sangre|January 1, 1981
[Blast crisis mimicking acute leukaemia as first manifestations of chronic myelogenous leukaemia. Report of three cases (author's transl)]F Cervantes, C Rozman, F Ballesta, et al.
American Journal of Medical Genetics|March 10, 2000
Paternal isodisomy 13 in a normal newborn infant after trisomy rescue evidenced by prenatal diagnosisA Soler, E Margarit, R Queralt, et al.
Medicina Clinica|July 30, 1999
[Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome]M Milà, A Carrió, A Sánchez, et al.
Biochemical and Biophysical Research Communications|May 8, 1998
Identification of conserved potentially regulatory sequences of the SRY gene from 10 different species of mammalsE Margarit, A Guillén, C Rebordosa, et al.
Pageof 7